Electron beam curable urethane resin for magnetic recording medium, method of manufacturing the same and magnetic recording medium using the same

ABSTRACT

An electron-beam curable polyurethane resin for magnetic recording media is produced by modifying a polyurethane resin having active hydrogen in the molecule thereof with a compound having at least two acrylic double bonds, wherein the modification is performed on the active hydrogen so that the polyurethane resin becomes electron-beam curable. By subjecting a known thermosetting polyurethane resin to electron-beam sensitive modification, the resulting resin is highly crosslinked and is thus capable of being suitably used for magnetic recording media. Also, an electron-beam curable polyurethane resin having excellent crosslinking characteristics can easily be produced from the known thermosetting polyurethane resin. Furthermore, by using the electron-beam curable polyurethane resin, a high-performance magnetic recording medium can be provided.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an electron-beam curable polyurethaneresin for magnetic recording media (hereinafter referred to as anelectron-beam curable resin in some cases), to a method for producingthe same, and to a magnetic recording medium using the same. Morespecifically, the present invention relates to an electron-beam curablepolyurethane resin having excellent crosslinking characteristics andwhich is suitably used for magnetic recording media, to a method forproducing the electron-beam curable polyurethane resin having excellentcrosslinking characteristics by electron-beam sensitive modification ofa common thermosetting polyurethane resin, and to a magnetic recordingmedium using the electron-beam curable polyurethane resin.

2. Description of the Related Art

Resins conventionally used for magnetic recording media typicallyinclude thermosetting resins and electron-beam curable resins. Thethermosetting resins are cured by allowing active hydrogen in theresins, which is typically the hydroxy group, to react with anisocyanate compound to form crosslinks in the resins. On the other hand,the electron-beam curable resins are cured by introducing anelectron-beam sensitive functional group, which is typically the acrylicdouble bond, and exposing the resins to an electron beam to formcrosslinks.

In general, vinyl chloride resins and polyurethane resins are used asthe electron-beam curable resins for magnetic recording media. Forelectron-beam sensitive modification of the vinyl chloride resins, thehydroxy group of a thermosetting vinyl chloride resin having a hydroxygroup may be allowed to react with a tolylene diisocyanate (TDI) adductproduced by a reaction between TDI and 2-hydroxyethyl methacrylate(2-HEMA) (disclosed in Japanese Examined Patent Application PublicationNo. 1-25141), allowed to react with a cyclic anhydride and further reactwith an epoxy monomer having an acrylic double bond (disclosed inJapanese Patent No. 2514682), or allowed to react with2-isocyanateethyl(meth)acrylate (MOI) (disclosed in Japanese UnexaminedPatent Application Publication NO. 4-67314).

On the other hand, in the case of using the polyurethane resins,typically, a (meth)acrylate compound having a hydroxy group in themolecule thereof may be used as part of the material for synthesizingpolyurethane to produce a radiation curable polyurethane resin(disclosed in Japanese Patent No. 2610468), or a polyurethane whosepolymer end is a isocyanate group may be prepared and subsequentlyallowed to react with an alcohol having an acrylic double bond(disclosed in Japanese Examined Patent Application Publication No.3-1727).

As for the electron-beam curable polyurethane resins, if an acrylicdouble bond can be introduced to the active hydrogen, which is typicallythe hydroxy group, of a known thermosetting polyurethane resin, in thesame manner as in the vinyl chloride resins, commercially availablepolyurethane resins can be modified to be electron-beam sensitive.

The thermosetting polyurethane resin however has a smaller amount ofactive hydrogen in the molecule thereof than that of thermosetting vinylchloride resins. Hence, when the modification is performed by the sametechnique as in the vinyl chloride resins, only a small number ofacrylic double bonds can be introduced and, consequently, crosslinkingof the coating film cured by electron-beam is disadvantageouslyinsufficient.

SUMMARY OF THE INVENTION

Accordingly, an object of the present invention is to provide anelectron-beam curable polyurethane resin having excellent crosslinkingcharacteristics and which is suitably used for magnetic recording media,by electron-beam sensitive modification of a known thermosettingpolyurethane resin, to provide a method for easily producing theelectron-beam curable polyurethane resin having excellent crosslinkingcharacteristics, from a known thermosetting polyurethane resin, and toprovide a high-performance magnetic recording medium by using theelectron-beam curable polyurethane resin.

The inventors of the present invention have conducted intensive researchto overcome the above-described challenges. Consequently, they havefound that an electron-beam curable polyurethane resin having excellentcrosslinking characteristics can be produced by using a knownpolyurethane resin as the raw material and modifying it with a compoundhaving at least two acrylic double bonds, and thus, accomplished thepresent invention.

Specifically, the electron-beam curable polyurethane resin for magneticrecording media, a method for producing the same, and a magneticrecording medium using the same are as follows.

(1) The electron-beam curable polyurethane resin for magnetic media isproduced by modifying a polyurethane resin having recording activehydrogen in the molecule thereof with a compound having at least twoacrylic double bonds, wherein the modification is performed on theactive hydrogen so that the polyurethane resin becomes electron-beamcurable.

(2) To produce the electron-beam curable polyurethane resin for magneticrecording media described in (1), in the method for producing theelectron-beam curable polyurethane resin for magnetic recording media,the active hydrogen of a polyurethane resin having active hydrogen inthe molecule thereof is allowed to react with a compound having at leasttwo acrylic double bonds and an isocyanate group in the moleculethereof, thereby being modified to be electron-beam curable.

(3) In the method described in (2), the compound is prepared by allowingan isocyanurate to react with an alcohol having at least one acrylicdouble bond in the molecule thereof.

(4) The magnetic recording medium comprises a non-magnetic substrateprovided with a layer containing the electron-beam curable polyurethaneresin for magnetic recording media described in (1).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The embodiments of the present invention will now be illustrated indetail.

The electron-beam curable polyurethane resin for magnetic recordingmedia of the present invention is produced by electron-beam sensitivemodification of a predetermined polyurethane resin, used as the rawmaterial, using a predetermined compound (hereinafter referred to as a“modifying compound”).

The raw material polyurethane resin used in the present invention may bea known (general-purpose) polyurethane resin or a newly developedpolyurethane resin. However, the polyurethane resin must have activehydrogen, such as the hydroxy group, primary amine, or secondary amine,in the molecule thereof in order to carry out reaction.

Such polyurethane resins are not particularly limited, but include, forexample, Estane 5776P, 5788P, and 5799P (produced by BF Goodrich Co.);UR8200, UR8300, and UR8700 (produced by Toyobo Co., Ltd); and N-2301,N-2304, N-3167, N-3301, N-4325, and TK501K (produced by NipponPolyurethane Industry Co., Ltd.).

As the modifying compound allowed to react with the active hydrogen ofthese polyurethane resins in order to carry out electron-beam sensitivemodification, a compound is used which has both at least two acrylicdouble bonds and an isocyanate group in the molecule thereof. Thismodifying compound can be prepared by, for example, allowing two of thethree isocyanate groups in a hexamethylene diisocyanate (HDI) trimer(isocyanurate) to react with a compound having both a hydroxy group andan acrylic double bond so as to have two acrylic double bonds and oneisocyanate group. The resulting modifying compound is allowed to reactwith, for example, the hydroxy group of a polyurethane resin. Thus, twoacrylic double bonds can be introduced for one hydroxy group of thepolyurethane resin.

The isocyanurate is not particularly limited, and other isocyanurates,such as of tolylene diisocyanate (TDI) and isophorone diisocyanate(IPDI) may be used instead of HDI. The compound allowed to react withthe isocyanurate nurato, having both a hydroxy group and at least oneacrylic double bond, that is, an alcohol having at least one acrylicdouble bond in the molecule thereof, is not particularly limited, andexemplary compounds include 2-hydroxyethyl acrylate (2-HEA),2-hydroxyethyl methacrylate (2-HEMA), 2-hydroxypropyl acrylate,hydroxydiethylene glycol methacrylate, butoxyhydroxypropyl acrylate,phenoxyhydroxypropyl acrylate, hydroxypropyl dimethacrylate, glyceroldimethacrylate, and monohydroxypentaerythritol triacrylate.

Synthesis of the electron-beam curable polyurethane resin is performedas described above, through a reaction of urethane formation betweenthree compounds consisting of the isocyanurate, the alcohol having atleast one acrylic double bond in the molecule thereof, and thepolyurethane resin having active hydrogen. As for the method for thesynthesis, preferably, the isocyanurate and the alcohol having at leastone acrylic double bond in the molecule thereof are precedently allowedto react with each other to prepare the above-described modifyingcompound, and then the polyurethane resin having active hydrogen isallowed to react.

In general, a catalyst for urethane formation, such as dibutyltindilaurate or tin octylate is preferably used in an amount of 0.005 to0.1 part by weight relative to 100 parts by weight in total ofreactants, In the synthesis. However, the catalyst for urethaneformation is not always necessary. The synthesis reaction temperature ispreferably 30 to 80° C., and more preferably 50 to 70° C.

The resulting electron-beam curable polyurethane resin can be used as abinder of a resin undercoat layer, an undercoat layer containing aninorganic pigment, a backcoat layer, and a magnetic layer, in a magneticrecording medium. Hereinafter, these layers are collectively referred toas “functional layers”. The electron-beam curable polyurethane resin maybe used singly or in combination with other resins such as vinylchloride resins.

Crosslinking of the electron-beam curable polyurethane resin isperformed with an electron-beam preferably at an exposure dose of 1 to10 Mrad, and more preferably 3 to 7 Mrad. The exposure energy(acceleration voltage) is preferably 100 kV or more.

In the present invention, by using the above-described electron-beamcurable polyurethane resin as a binder of the functional layers, ahigh-performance magnetic recording medium can be obtained whichincludes highly crosslinked, highly solvent-resistant functional layers.The magnetic recording medium of the present invention needs to have alayer containing the electron-beam curable polyurethane resin of thepresent invention on a non-magnetic substrate. However, the otherconstruction materials and additives are not particularly limited, andthe following materials may be used.

The material of the non-magnetic substrate may appropriately be selectedfrom known resin films, such as polyester, polyamide, and aromaticpolyamide, and laminates of these resin films. The thickness of thesubstrate is in a known range, and is also not particularly limited.

The ferromagnetic powder used for the magnetic layer is acicularferromagnetic metallic powder having a mean long-axis length ofpreferably 0.15 μm or less, and more preferably 0.05 to 0.10 μm. If themean long-axis length is more than 0.15 μm, electromagnetic conversioncharacteristics (particularly S/N and C/N ratios) required for magneticrecording media tend not to be satisfied. Alternatively, a hexagonaliron oxide powder, such as barium ferrite, may be used. The platy ratioof the hexagonal iron oxide powder is preferably 2 to 7. Also, the meanprimary plate diameter is preferably 10 to 50 nm when observed by TEM.If it is large, the surface of the magnetic layer tends to deteriorate.

It is sufficient that the magnetic layer composition contains 70 to 90percent by weight of such ferromagnetic powder. An excessively highcontent of the ferromagnetic powder results in a low content of thebinder, and consequently the surface smoothness by calendaring is liableto deteriorate. In contrast, an excessively low content of theferromagnetic powder tends not to provide a high reproduction output.

Preferred binder resins for the magnetic layer include the electron-beamcurable polyurethane resin of the present invention, known thermoplasticresins and thermosetting resins, other radiation curable resins, andtheir mixtures, but are not particularly limited to these. Also, amixture of the electron-beam curable polyurethane resin of the presentinvention and other binder resins may be used.

The content of the binder resin used for the magnetic layer is 5 to 40parts by weight relative to 100 parts by weight of the ferromagneticpowder, and a content of 10 to 30 parts by weight is particularlypreferable. An excessively low content of the binder resin degrades thestrength of the magnetic layer and consequently the running durabilitytents to deteriorate. In contrast, an excessively high content resultsin a reduced content of the ferromagnetic metallic powder content,consequently degrading electromagnetic conversion characteristics.

Cross-linkers for curing the binder resin include known various types ofpolyisocyanate, and the cross-linker content is preferably 10 to 30parts by weight relative to 100 parts by weight of the binder resin. Themagnetic layer may also contain an abrasive, a dispersant such as asurfactant, a higher fatty acid, and other additives, if necessary.

A paint for magnetic layer formation is prepared by adding an organicsolvent to the above-described ingredients. The organic solvent is notparticularly limited, and may be at least one appropriately selectedfrom among various solvents including ketones, such as methyl ethylketone (MEK), methyl isobutyl ketone, and cyclohexanone, and aromaticsolvents, such as toluene. The organic solvent content is about 100 to900 parts by weight relative to 100 parts by weight in total of solids(the ferromagnetic metallic powder, various types of inorganic grains,and the like) and the binder resin.

The thickness of the magnetic layer, in the present invention, is 0.50μm or less, preferably 0.01 to 0.50 μm, and more preferably 0.02 to 0.30μm. An excessively large thickness leads to an increasedself-demagnetization loss and thickness loss.

A non-magnetic layer serving as the undercoat layer may be disposedbetween the magnetic layer and the non-magnetic substrate, therebyimproving electromagnetic conversion characteristics of the magneticlayer having a reduced thickness. Thus, reliability is furtherincreased.

Various types of inorganic powder can be used as the non-magnetic powderfor the non-magnetic layer, and preferred inorganic powders includeacicular nonmagnetic powders, such as acicular non-magnetic iron oxide(α-Fe₂O₃). The non-magnetic layer may further contain various types ofnon-magnetic powder, such as calcium carbonate (CaCO₃), titanium oxide(TiO₂), barium sulfate (BaSO4), and α-alumina (α-Al₂O₃), if necessary.Preferably, the nonmagnetic layer contains carbon black. The carbonblack may be furnace black for rubber, thermal black for rubber, blackfor color, acetylene black, and the like.

The compounding ratio of the carbon black to the inorganic powder ispreferably 100:0 to 10:90 by weight. If the inorganic powder ratio ismore than 90, a problem of surface electric resistance is liable tooccur.

Exemplary binders for the nonmagnetic layer include the electron-beamcurable polyurethane of the present invention, known thermoplasticresins and thermosetting resins, other radiation curable resins, andtheir mixtures, as In the magnetic layer, and the radiation curableresins are particularly suitable.

The non-magnetic layer may further contain a dispersant such as asurfactant and other additives, if necessary. The paint for thenon-magnetic layer may be prepared by adding the same organic solvent asin the above-described magnetic layer in a similar amount.

The thickness of the non-magnetic layer is preferably 2.5 μm or less,and more preferably 0.1 to 2.3 μm. Even if the thickness is increased tomore than 2.5 μm, performance is not enhanced. On the contrary, strictconditions are required for coating because the thickness of the coatingis liable to become nonuniform, and the surface smoothness is alsoliable to deteriorate.

The backcoat layer is intended to enhance the running stability and toprevent electrification of the magnetic layer, and is provided ifrequired. Preferably, the backcoat layer contains 30 to 80 percent byweight of carbon black. As the carbon black, any type can be used aslong as it is generally used, and the same carbon black as in theabove-described non-magnetic layer may be used. In addition to thecarbon black, the backcoat layer may further contain various types ofnon-magnetic, inorganic powder used for the magnetic layer, such as anabrasive; a dispersant such as a surfactant; a higher fatty acid; afatty ester; a lubricant, such as silicone oil, and other various typesof additives.

The thickness (after calendaring) of the backcoat layer is 0.1 to 1.0μm, and preferably 0.2 to 0.8 μm. If the thickness is more than 1.0 μm,the friction between a medium-sliding path and the medium becomesexcessively large, and consequently the running stability tends todeteriorate. In contrast, in the case of a thickness of less than 0.1μm, the coating of the backcoat layer is liable to be shaved off whilethe medium is running.

As described above, according to the present invention, an electron beamcurable polyurethane resin for magnetic recording media can be producedusing a known polyurethane resin having active hydrogen as the rawmaterial. The resulting electron-beam curable polyurethane resin hasexcellent crosslinking characteristics, and thus a high-performancerecording magnetic medium can be provided.

EXAMPLES

The present invention will further be described in detail usingexamples. However, the examples do not limit the present invention. Inthe following description, “part(s)” refers to “part(s) by weight”.

Synthesis Example 1 Polyurethane Acrylate Resin (1)

A one litter, three-neck flask was charged with 504 parts of HDI nurate,0.18 part of dibutyltin dilaurate, and 0.22 part of2,6-tert-butyl-4-methylphenol (BHT), and 232 parts of 2-hydroxyethylacrylate was dripped while temperature was controlled to 60° C. Afterdripping, the sample was stirred at 60° C. for 2 hours and taken out.Thus, HDI nurate-2-HEA adduct (modifying compound) was obtained.

Next, 262 parts of Estane 5778P produced by BP Goodrich Co., 700 partsof methyl ethyl ketone (MEK), 0.5 part of dibutyltin dilaurate, and 0.05part of 2,6-tert-butyl-4-methylphenol (BHT) were compounded and stirredat 70° C. for 3 hours. Then, 38 parts of the previously prepared HDInurate-2-HEA adduct (modifying compound) was added. After stirring at70° C. for 15 hours, it was made sure that the isocyanate characteristicabsorption peak (2270 cm⁻¹) had disappeared in the IR spectrum, and thenthe sample was taken out. Thus, polyurethane acrylate resin (1) wasobtained.

Synthesis Example 2 Polyurethane Acrylate Resin (2)

A one litter, three-neck flask was charged with 504 parts of HDI nurate,0.18 part of dibutyltin dilaurate, and 0.22 part of2,6-tert-butyl-4-methylphenol (BHT), and 260 parts of 2-hydroxyethylmethacrylate (2-HEMA) was dripped while temperature was controlled to60° C. After dripping, the sample was stirred at 60° C. for 2 hours andtaken out. Thus, HDI nurate-2-HEMA adduct (modifying compound) wasobtained.

Next, 262 parts of Estane 5778P produced by BF Goodrich Co., 700 partsof MEK, 0.5 part of dibutyltin dilaurate, and 0.05 part of2,6-tert-butyl-4-methylphenol (BHT) were compounded and stirred at 70°C. for 3 hours. Then, 40 parts of the previously prepared HDInurate-2-HEMA adduct (modifying compound) was added. After stirring at70° C. for 15 hours, it was made sure that the isocyanate characteristicabsorption peak (2270 cm⁻¹) had disappeared in the IR spectrum, and thenthe sample was taken out. Thus,

Synthesis Example 3 Polyurethane Acrylate Resin (3)

A one litter, three-neck flask was charged with 504 parts of HDI nurate,0.18 part of dibutyltin dilaurate, and 0.22 part of2,6-tert-butyl-4-methylphenol, and 496 parts ofmonohydroxypentaerythritol triacrylate was dropped while temperature wascontrolled to 60° C. After dripping, the sample was stirred at 60° C.for 2 hours and taken out. Thus, HDI nurate-monohydroxypentaerythritoltriacrylate adduct (modifying compound) was obtained.

Next, 230 parts of Estane 5778P produced by BF Goodrich Co., 615 partsof MEK, 0.5 part of dibutyltin dilaurate, and 0.05 part of2,6-tert-butyl-4-methylphenol (BHT) were compounded and stirred at 70°C. for 3 hours. Then, 53 parts of the previously prepared HDInurate-monohydroxypentaerythritol triacrylate adduct (modifyingcompound) was added. After stirring at 70° C. for 15 hours, it was madesure that the isocyanate characteristic absorption peak (2270 cm⁻¹) haddisappeared in the IR spectrum, and then the sample was taken out. Thus,polyurethane acrylate resin (3) was obtained.

Synthesis Example 4 Polyurethane Acrylate Resin (4)

A one litter, three-neck flask was charged with 333 parts of IPDInurate, 450 parts of MEK, 0.44 part of dibutyltin dilaurate, and 0.27part of 2,6-tert-butyl-4-methylphenol (BHT), and 116 parts of2-hydroxyethyl acrylate (2-HEA) was dripped while temperature wascontrolled to 60° C. After dripping, the sample was stirred at 60° C.for 5 hours and taken out. Thus, IPDI nurate-2-HEA adduct (modifyingcompound) was obtained.

Next, 254 parts of Estane 5778P produced by BF Goodrich Co., 654 partsof MEK, 0.5 part of dibutyltin dilaurate, and 0.05 part of2,6-tert-butyl-4-methylphenol (BHT) were compounded and stirred at 70°C. for 3 hours. Then, 92 parts of the previously prepared TPDTnutrate-2-HEA adduct (modifying compound) was added. After stirring at70° C. for 15 hours, it was made sure that the isocyanate characteristicabsorption peak (2270 cm⁻¹) had disappeared in the IR spectrum, and thenthe sample was taken out. Thus, polyurethane acrylate resin (4) wasobtained.

Synthesis Example 5 Polyurethane Acrylate Resin (5)

In a one litter, three-neck flask, 833 parts of Vylon UR8300 produced byToyobo Co., Ltd., 0.5 part of dibutyltin dilaurate, and 0.05 part of2,6-tert-butyl-4-methylphenol (BHT) were placed and stirred at 70° C.for 1 hours. Then, 13 parts of the previously prepared HDI nurate-2-HEAadduct (modifying compound) was added. After stirring at 70° C. for 15hours, it was made sure that the isocyanate characteristic absorptionpeak (2270 cm⁻¹) had disappeared in the IR spectrum, and then the samplewas taken out. Thus, polyurethane acrylate resin (5) was obtained.

Synthesis Example 6 Polyurethane Acrylate Resin (6)

In a one litter, three-neck flask, 230 parts of Estane 5778P produced byBF Goodrich Co., 520 parts of MEK, 0.5 part of dibutyltin dilaurate, and0.3 part of hydroquinone were placed and stirred at 70° C. for 3 hours.Then, 8 parts of 2-isocyanateethyl methacrylate was added. Afterstirring at 70° C. for 15 hours, it was made sure that the isocyanatecharacteristic absorption peak (2270 cm⁻¹) had disappeared in the IRspectrum, and then the sample was taken out. Thus, polyurethane acrylateresin (6) was obtained.

Synthesis Example 7 Polyurethane Acrylate Resin (7)

A one litter, three-neck flask was charged with 348 parts of tolylenediisocyanate (TDI) and heated to 80° C. Then, 260 parts of2-hydroxyethyl methacrylate (2-HEMA), 0.07 part of tin octylate, and0.05 part of hydroquinone were dripped while temperature was controlledto 80° C. After dripping, the sample was stirred at 80° C. for 3 hoursand taken out. Thus, TDI-2-HEMA adduct was obtained.

Next, 226 parts of Estane 5778P produced by BF Goodrich Co., 560 partsof MEK, 0.5 part of dibutyltin dilaurate, and 0.05 part of2,6-tert-butyl-4-methylphenol (BHT) were compounded and stirred at 80°C. for 3 hours. Then, 14 parts of the previously prepared TDI-2-HEMAadduct was added. After stirring at 80° C. for 15 hours, it was madesure that the isocyanate characteristic absorption peak (2270 cm⁻¹) haddisappeared in the IR spectrum, and then the sample was taken out. Thus,polyurethane acrylate resin (7) was obtained.

Synthesis Example 8 Polyurethane Acrylate Resin (8)

In a one litter, three-neck flask, 200 parts of Estane 5778P produced byBF Goodrich Co. and 525 parts of MEK were placed and stirred at 80° C.for 3 hours. Then, 6 parts of 1,2-cyclohexanedicarboxylic anhydride wasadded and allowed to react at 80° C. until the anhydride characteristicabsorption peaks (1790 cm⁻¹ and 1870 cm⁻¹) disappeared. Furthermore, 12parts of 1,2-cyclohexanedicarboxylic anhydride, 17 parts of glycidylmethacrylate, 0.02 part of hydroquinone, and 0.1 part of triethanolaminewere slowly added and stirred at 80° C. for 20 hours. Then, it was madesure that the acid value was 4 or less, and the sample was taken out toobtain polyurethane acrylate resin (8).

Example 1

Evaluation 1: Evaluation of Crosslinking Characteristics

A coating of polyurethane acrylate resin (1) was formed to a thicknessof 30 μm on a separation film, and was then exposed to an electron beamof 6 Mrad under the condition of an acceleration voltage of 200 kV to becured. Next, the polyurethane resin coating film cured with electronbeam was removed from the separation film, and the gel fraction wasmeasure under the following conditions.

<Gel Fraction Measurement Conditions>

Solvent: methyl ethyl ketone (MEK)

Extraction condition: boiling in MEK

Extraction time: 5 hours

Extraction was performed under the conditions above. The polyurethaneresin coating film was weighed before and after the extraction, and thegel fraction was calculated from the difference between the obtainedweights.

Evaluation 2: Evaluation of Crosslinking Characteristics of CoatingFilms Containing Pigment or Magnetic Powder

For three types of coating, a magnetic metallic powder (magnetic paint),an α-iron oxide/carbon black mixture (non-magnetic paint), and a carbonblack (carbon black paint) were each dispersed in polyurethane acrylateresin (1), and crosslinks were formed. Solvent resistances of thesesamples were evaluated to estimate crosslinking characteristics.

(1) Evaluation of Magnetic Metallic Powder

Preparation of Magnetic Paint Sample Magnetic metallic powder 100 partsby weight (Fe/Co/Al/Y = 100/10/5.2/2.0 (by weight): (Hc = 144.6 kA/m(1830 Oe), σs = 130 Am²/kg, BET = 57 m²/g, mean long-axis length = 0.10μm) Polyurethane acrylate resin (1): 70 parts by weight MEK: 70 parts byweight Toluene: 120 parts by weight Cyclohexanone: 70 parts by weight

After being mixed and kneaded, these ingredients were dispersed with asand grinder mill to prepare a magnetic paint.

Next, the resulting magnetic paint was applied on a polyethyleneterephthalate (PET) film having a thickness of 6.1 μm so as to result ina dried thickness of 1.5 μm. After drying at a temperature of 100° C.calendaring was performed at a linear pressure of 2.9×10⁵ N/m and atemperature of 90° C. and subsequently electron beam (EB) exposure (6Mrad) was performed. Thus, a cured magnetic coating film was prepared.

(2) Evaluation of α-Iron Oxide/Carbon Black Pigment Mixture

Preparation of Non-Magnetic Paint Sample Non-magnetic powder: acicularα-Fe₂O₃: 80 parts by weight (mean short-axis diameter: 18 nm, aspectratio: 6.1, pH: 8.9) Carbon black (#850B produced by Mitsubishi 20 partsby weight Chemical Co.): (mean particle size: 16 nm, BET: 200 m²/g, DBPoil absorption: 70 mL/100 g) Polyurethane acrylate resin (1): 70 partsby weight MEK: 120 parts by weight Toluene: 120 parts by weightCyclohexanone: 70 parts by weight

After being mixed and kneaded, these ingredients were dispersed with asand grinder mill to prepare a non-magnetic paint.

Next, the resulting non-magnetic paint was applied on a PET film havinga thickness of 6.1 μm so as to result in a dried thickness of 1.5 μm.After drying at a temperature of 100° C., calendaring was performed at alinear pressure of 2.9×10⁵ N/m and a temperature of 90° C. andsubsequently EB exposure (6 Mrad) was performed. Thus, a curednon-magnetic coating film was prepared.

(3) Evaluation of Carbon Black Type

Preparation of Carbon Black Paint Sample Carbon black: 100 parts byweight (Conductex SC produced by Columbian Carbon Co., mean particlesize: 20 nm, BET: 220 m²/g) Carbon black: 1 part by weight (Sevacarb MTproduced by Columbian Carbon Co., mean particle size: 350 nm, BET: 8m²/g) Polyurethane acrylate resin (1): 330 parts by weight MEK: 350parts by weight Toluene: 350 parts by weight Cyclohexanone: 170 parts byweight

After being mixed and kneaded, these ingredients were dispersed with asand grinder mill.

Next, the resulting carbon black paint was applied on a PET film havinga thickness of 6.1 μm so as to result in a dried thickness of 1.5 μm.After drying at a temperature of 100° C., calendaring was performed at alinear pressure of 2.9×10⁵ N/m and a temperature of 70° C. andsubsequently EB exposure (6 Mrad) was performed. Thus, a cured carbonblack coating film was prepared.

The solvent resistances of the film samples prepared in theabove-described manner were evaluated according to the followingprocedure and criteria.

1. A cotton swab impregnated with MEK was used.

2. The surfaces of the films were rubbed with the cotton swab.

3. It was counted how many times of rubbing were performed before thefilm disappeared.

4. 10 times or more: good

5 to 10 times: fair

1 to 5 times: bad

Example 2

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (2) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Example 3

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (3) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Example 4

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (4) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Example 5

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (5) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Comparative Example 1

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (6) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Comparative Example 2

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (7) was used Instead of polyurethaneacrylate resin (1) used in Example 1.

Comparative Example 3

Coating film samples were prepared and the gel fractions and solventresistances were evaluated, in an identical manner to Example 1 exceptthat polyurethane acrylate resin (8) was used instead of polyurethaneacrylate resin (1) used in Example 1.

Comparative Example 4

In 700 g of MEK, 300 g of Estane 5778P produced by BF Goodrich Co. wasdissolved to prepare a polyurethane resin solution. Coating film sampleswere prepared and the gel fractions and solvent resistances wereevaluated, in an identical manner to Example 1 except that thispolyurethane resin solution was used instead of polyurethane acrylateresin (1) used in Example 1. TABLE 1 Solvent resistance Non- Carbon GelMagnetic magnetic black fraction coating coating coating Resin (%) filmfilm film Example 1 Polyurethane 96 Good Good Good acrylate resin (1)Example 2 Polyurethane 95 Good Good Good acrylate resin (2) Example 3Polyurethane 98 Good Good Good acrylate resin (3) Example 4 Polyurethane96 Good Good Good acrylate resin (4) Example 5 Polyurethane 85 Good-Good- Good- acrylate resin Fair Fair Fair (5) Comparative Polyurethane20 Bad Bad Bad Example 1 acrylate resin (6) Comparative Polyurethane 5Bad Bad Bad Example 2 acrylate resin (7) Comparative Polyurethane 5 BadBad Bad Example 3 acrylate resin (8) Comparative Polyurethane 0 Bad BadBad Example 4 resin solution

According to the results shown in Table 1 above it has been shown thatthe polyurethane resins of the examples produced by modifying apolyurethane resin having active hydrogen with a compound having two ormore of acrylic double bonds and an isocyanate group in the moleculethereof have more excellent crosslinking characteristics than those ofthe known polyurethane resin used in the comparative examples and canresult in cured coating films having better solvent resistance to amagnetic paint, a non-magnetic paint, and a black carbon paint.

1-20. (canceled)
 21. An electron-beam curable polyurethane resin for amagnetic recording medium comprising an isocyanurate having two acrylicdouble bonds.
 22. The electron-beam curable polyurethane resin for amagnetic recording medium of claim 21, wherein the isocyanurate isdelivered by a trimer of isophorone diisocyanate.
 23. The electron-beamcurable polyurethane resin for a magnetic recording medium of claim 21,wherein the isocyanurate is delivered by an alcohol having at least oneacrylic double bond.
 24. A magnetic recording medium comprising theelectron-beam curable polyurethane resin of claim
 21. 25. The magneticrecording medium of claim 24, further comprising a non-magneticsubstrate provided with a layer containing the electron-beam curablepolyurethane resin.